US7235264B2 - Cerebral protection with a gas comprising xenon - Google Patents
Cerebral protection with a gas comprising xenon Download PDFInfo
- Publication number
- US7235264B2 US7235264B2 US10/517,723 US51772304A US7235264B2 US 7235264 B2 US7235264 B2 US 7235264B2 US 51772304 A US51772304 A US 51772304A US 7235264 B2 US7235264 B2 US 7235264B2
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- US
- United States
- Prior art keywords
- xenon
- medicament
- volume
- gas
- cerebral
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 229910052724 xenon Inorganic materials 0.000 title claims abstract description 165
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 title claims abstract description 165
- 230000002490 cerebral effect Effects 0.000 title claims abstract description 35
- 230000004224 protection Effects 0.000 title claims abstract description 26
- 239000003814 drug Substances 0.000 claims abstract description 101
- 239000007789 gas Substances 0.000 claims abstract description 87
- 230000006735 deficit Effects 0.000 claims abstract description 17
- 230000003788 cerebral perfusion Effects 0.000 claims abstract description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 65
- 239000001301 oxygen Substances 0.000 claims description 65
- 229910052760 oxygen Inorganic materials 0.000 claims description 65
- 239000000203 mixture Substances 0.000 claims description 36
- 238000011282 treatment Methods 0.000 claims description 28
- 210000004556 brain Anatomy 0.000 claims description 26
- 238000002360 preparation method Methods 0.000 claims description 9
- 239000011261 inert gas Substances 0.000 claims description 8
- 208000006011 Stroke Diseases 0.000 claims description 6
- 230000017531 blood circulation Effects 0.000 claims description 6
- 230000000241 respiratory effect Effects 0.000 claims description 6
- 230000024883 vasodilation Effects 0.000 claims description 5
- 208000028867 ischemia Diseases 0.000 claims description 3
- 230000001737 promoting effect Effects 0.000 claims description 3
- 208000011580 syndromic disease Diseases 0.000 claims description 3
- 238000000034 method Methods 0.000 claims 7
- 238000011321 prophylaxis Methods 0.000 abstract description 13
- 208000018152 Cerebral disease Diseases 0.000 abstract description 7
- 238000002560 therapeutic procedure Methods 0.000 abstract description 5
- 230000001149 cognitive effect Effects 0.000 abstract description 4
- 230000001953 sensory effect Effects 0.000 abstract description 3
- 230000010412 perfusion Effects 0.000 abstract description 2
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 116
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 72
- 229910052757 nitrogen Inorganic materials 0.000 description 36
- 150000001875 compounds Chemical class 0.000 description 12
- 239000000126 substance Substances 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 9
- 238000009423 ventilation Methods 0.000 description 6
- 230000004936 stimulating effect Effects 0.000 description 5
- 229940124549 vasodilator Drugs 0.000 description 5
- 239000003071 vasodilator agent Substances 0.000 description 5
- 206010021143 Hypoxia Diseases 0.000 description 4
- 208000010877 cognitive disease Diseases 0.000 description 4
- 239000013066 combination product Substances 0.000 description 4
- 229940127555 combination product Drugs 0.000 description 4
- 230000007774 longterm Effects 0.000 description 4
- 208000012902 Nervous system disease Diseases 0.000 description 3
- 206010047141 Vasodilatation Diseases 0.000 description 3
- 239000000443 aerosol Substances 0.000 description 3
- 230000003931 cognitive performance Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000004089 microcirculation Effects 0.000 description 3
- 210000002569 neuron Anatomy 0.000 description 3
- 230000004112 neuroprotection Effects 0.000 description 3
- 230000002792 vascular Effects 0.000 description 3
- 206010002091 Anaesthesia Diseases 0.000 description 2
- 208000028698 Cognitive impairment Diseases 0.000 description 2
- 102000004868 N-Methyl-D-Aspartate Receptors Human genes 0.000 description 2
- 108090001041 N-Methyl-D-Aspartate Receptors Proteins 0.000 description 2
- 208000026301 Postoperative Cognitive Complications Diseases 0.000 description 2
- ZIIQCSMRQKCOCT-YFKPBYRVSA-N S-nitroso-N-acetyl-D-penicillamine Chemical compound CC(=O)N[C@@H](C(O)=O)C(C)(C)SN=O ZIIQCSMRQKCOCT-YFKPBYRVSA-N 0.000 description 2
- UJLFQHSVIUGIOA-UHFFFAOYSA-N [O].[Xe] Chemical compound [O].[Xe] UJLFQHSVIUGIOA-UHFFFAOYSA-N 0.000 description 2
- 230000037005 anaesthesia Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000000747 cardiac effect Effects 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 210000004072 lung Anatomy 0.000 description 2
- 230000007102 metabolic function Effects 0.000 description 2
- 230000035771 neuroregeneration Effects 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- WTLKTXIHIHFSGU-UHFFFAOYSA-N 2-nitrosoguanidine Chemical compound NC(N)=NN=O WTLKTXIHIHFSGU-UHFFFAOYSA-N 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- ODKSFYDXXFIFQN-BYPYZUCNSA-N L-arginine Chemical compound OC(=O)[C@@H](N)CCCN=C(N)N ODKSFYDXXFIFQN-BYPYZUCNSA-N 0.000 description 1
- 229930064664 L-arginine Natural products 0.000 description 1
- 235000014852 L-arginine Nutrition 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- SNIOPGDIGTZGOP-UHFFFAOYSA-N Nitroglycerin Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 description 1
- XOWVFANEOZMPKG-REOHCLBHSA-N S-nitroso-L-cysteine Chemical compound OC(=O)[C@@H](N)CSN=O XOWVFANEOZMPKG-REOHCLBHSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- YEESUBCSWGVPCE-UHFFFAOYSA-N azanylidyneoxidanium iron(2+) pentacyanide Chemical compound [Fe++].[C-]#N.[C-]#N.[C-]#N.[C-]#N.[C-]#N.N#[O+] YEESUBCSWGVPCE-UHFFFAOYSA-N 0.000 description 1
- 150000001540 azides Chemical class 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 230000008499 blood brain barrier function Effects 0.000 description 1
- 210000004204 blood vessel Anatomy 0.000 description 1
- 210000001218 blood-brain barrier Anatomy 0.000 description 1
- 230000036760 body temperature Effects 0.000 description 1
- 239000002327 cardiovascular agent Substances 0.000 description 1
- 229940125692 cardiovascular agent Drugs 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000003728 cerebral autoregulation Effects 0.000 description 1
- 230000003727 cerebral blood flow Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 229940124645 emergency medicine Drugs 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 238000002695 general anesthesia Methods 0.000 description 1
- OWFXIOWLTKNBAP-UHFFFAOYSA-N isoamyl nitrite Chemical compound CC(C)CCON=O OWFXIOWLTKNBAP-UHFFFAOYSA-N 0.000 description 1
- 229940075473 medical gases Drugs 0.000 description 1
- 239000002207 metabolite Substances 0.000 description 1
- 229960002460 nitroprusside Drugs 0.000 description 1
- 231100000957 no side effect Toxicity 0.000 description 1
- 238000006213 oxygenation reaction Methods 0.000 description 1
- 230000000069 prophylactic effect Effects 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 230000029058 respiratory gaseous exchange Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P39/00—General protective or antinoxious agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Definitions
- the invention relates to a medicament which comprises xenon and, where appropriate, an NO source.
- WO 02/22141 A2 describes the use of xenon or xenon-containing gases as medicament, in particular cardiovascular agent.
- Neuroprotection and neuroregeneration involves the protection and the regeneration of individual nerve cells by acting on NMDA receptors in the nerve cell. Neuroprotection by modulating the activity of NMDA receptors is also disclosed in U.S. Pat. No. 6,274,633.
- An undersupply of oxygen to the brain leads to damage to the brain.
- the invention is based on the object of providing an alternative medicament, in particular a medicament for the treatment of cerebral disorders.
- the invention relates to a medicament for cerebral protection having the features described in claim 1 .
- Cerebral protection is defined as reducing or preventing impairments of cerebral function of various causes, but especially secondary to perfusion impairments of unclear etiology.
- the medicament can be used for cerebral protection for the prophylaxis of impairments of cerebral perfusion and for therapy after cerebral disorders have occurred, irrespective of the cause (e.g. cognitive, sensory or motor in nature).
- the medicament for cerebral protection protects the brain of humans or mammals from damage, in particular from damage associated with oxygen deficiency. It does not act just on single nerve cells but acts on the brain or on parts of the brain.
- the medicament for cerebral protection acts in particular on the blood vessels in the brain.
- Available results indicate an improvement in cerebral perfusion through administered xenon.
- xenon acts as vasodilator, especially as capillary vasodilator in the capillary vascular system.
- cerebral autoregulation is maintained or improved.
- the oxygen supply in the brain is increased.
- the invention thus relates further to the use of xenon or of a xenon-containing gas as cerebral vasodilator, preferably as cerebral capillary vasodilator, in particular as cerebral capillary vasodilator in the capillary vascular system.
- the invention further relates to the use of xenon or of a xenon-containing gas to produce a medicament for cerebral vasodilatation, preferably to produce a medicament for cerebral capillary vasodilatation, in particular to produce a medicament for cerebral capillary vasodilatation in the capillary vascular system.
- Xenon or a xenon-containing gas mixture are further used to produce a medicament for the treatment of impairments of blood flow in the brain, to produce a medicament for the treatment of impairment of cerebral perfusion, to produce a medicament for the treatment of cognitive impairments, to produce a medicament for cerebral protection, to produce a medicament for the prophylaxis and/or therapy of impairments of cognitive performance, also postoperatively, to produce a medicament for the treatment of stroke, to produce a medicament for the prophylaxis of stroke, to produce a medicament for improving the oxygen supply in the brain, to produce a medicament for the treatment of post-ischemia syndrome, to produce a medicament for promoting blood flow in the brain.
- xenon or xenon-containing gas mixtures are advantageously employed as medicament for the treatment of states with oxygen deficiency, especially oxygen deficiency in the brain.
- xenon or xenon-containing gas mixtures are employed in emergency situations such as the treatment of avalanche victims.
- Xenon or a xenon-containing gas mixture is also used to produce a medicament for improving the oxygenation of the brain.
- Xenon or a xenon-containing gas mixture are further used to produce a medicament for the treatment of cognitive or cerebral dysfunction, in particular of postoperative cognitive dysfunction after cardiac surgical operations, also with use of heart-lung machines (HLM) and cardiac assist systems after general surgical procedures.
- HLM heart-lung machines
- Cerebral dysfunctions relate to impairments of the microcirculation, of oxygen utilization and of metabolic functions.
- the medicament is thus also used to treat cerebral disorders such as impairments of the microcirculation, of oxygen utilization and of metabolic functions.
- the medicament effects an increase in the cerebral blood flow and the microcirculation.
- the invention thus further relates to the use of xenon or of a xenon-containing gas mixture to produce a medicament for the treatment of cognitive dysfunction, in particular of postoperative cognitive dysfunction.
- the invention further relates to the use of xenon or of a xenon-containing gas mixture to produce a medicament for the treatment of cerebral dysfunction.
- the medicament for cerebral protection and the indications mentioned comprises xenon or a xenon-containing gas mixture. It preferably consists of gaseous xenon or a xenon-containing gas mixture.
- the medicament consists for example of xenon gas, a gas mixture of xenon and oxygen or a gas mixture of xenon, oxygen and an inert gas.
- the medicament for cerebral protection and the indications mentioned (referred to as the medicament for short) is preferably gaseous, in particular it contains no solid or liquid constituents on administration, and is thus preferably in the form of a pure gas phase on administration.
- the medicament for cerebral protection and the indications mentioned is preferably administered by inhalation through the lungs.
- the medicament is also administered by means of a heart-lung machine.
- the medicament is preferably used for treating humans.
- the medicament for cerebral protection and the indications mentioned is usually provided as pure gaseous xenon. It may also be provided as gas mixture.
- the medicament is usually employed as a gas mixture which maintains respiration and which comprises xenon and oxygen. Such gas mixtures are employed for example in emergency medicine, where gas-mixing or gas-metering devices are too complicated for mobile use.
- Gaseous xenon or xenon-containing gas mixtures are particularly advantageously employed for prophylaxis. Prophylactic administration of xenon or xenon-containing gas mixtures takes place for example preoperatively, intraoperatively or postoperatively.
- the provided medicament for cerebral protection and the indications mentioned, or the medicament produced directly on use, in particular in the direct vicinity of the patient is for example a gas mixture which comprises from 1 to 80% by volume (based on standard conditions, i.e. 20° C., 1 bar absolute) xenon (e.g. remainder oxygen).
- the medicament which is administered to the patient comprises xenon in pharmacologically or therapeutically effective amount, in particular in subanesthetically or anesthetically effective amount.
- a medicament with xenon in subanesthetically effective amount is advantageous.
- Subanesthetically effective (subanesthetic) amounts of xenon mean those amounts or concentrations of xenon which are insufficient for general anesthesia.
- xenon in general amounts of up to 70% by volume xenon, preferably up to 65% by volume, particularly preferably up to 60% by volume, in particular up to 50% by volume xenon.
- Pure xenon is accordingly metered into the patient's respiratory gas in the stated concentrations.
- the respiratory gas supplied to the patient comprises for example from 5 to 60% by volume, 5 to 50% by volume, 5 to 40% by volume, 5 to 30% by volume or 5 to 20% by volume xenon.
- a dosage of xenon in the respiratory gas with a low concentration for example 1 to 35% by volume, 5 to 25% by volume or 5 to 20% by volume xenon in the respiratory gas, may be advantageous.
- the medicaments in particular gaseous medicaments, preferably comprise besides xenon one or more gases or substances which are gaseous at body temperature under atmospheric pressure.
- gas mixtures which can be used are xenon-oxygen gas mixtures or gas mixtures of xenon and one or more inert gases such as nitrogen or a rare gas or xenon-oxygen inert gas gas mixtures. Admixture of a gas to the xenon may be very advantageous if it is intended to introduce little xenon into the body.
- gases or gas mixtures employed as medicament for cerebral protection 1.) 100% by volume xenon; 2.) 70% by volume xenon/30% by volume oxygen; 3.) 65% by volume xenon/30% by volume oxygen/5% by volume nitrogen; 4.) 65% by volume xenon/35% by volume oxygen; 5.) 60% by volume xenon/30% by volume oxygen/10% by volume nitrogen; 6.) 60% by volume xenon/35% by volume oxygen/5% by volume nitrogen; 7.) 60% by volume xenon/40% by volume oxygen; 8.) 55% by volume xenon/25% by volume oxygen/20% by volume nitrogen; 9.) 55% by volume xenon/30% by volume oxygen/15% by volume nitrogen; 10.) 55% by volume xenon/35% by volume oxygen/10% by volume nitrogen; 11.) 55% by volume xenon/40% by volume oxygen/5% by volume nitrogen; 12.) 55% by volume xenon/45% by volume oxygen; 13.) 50% by volume xenon/50% by volume oxygen; 14.) 50% by volume xenon; 3.
- the medicament is particularly advantageously employed in intensive-care medicine, especially when the medicament must be administered over a prolonged period, for example during long-term ventilation.
- the medicament has the particular advantage according to the current state of knowledge of having no side effects because the medicament itself is not metabolized by the body.
- no metabolites are formed in the body, and no accumulation of the medicament in the body occurs.
- Xenon is administered, especially during long-term ventilation and for prophylaxis, advantageously in subanesthetically effective concentrations in a breathable gas (respiratory gas).
- Administration of breathable gases with a content of from 5 to 45% by volume xenon, preferably 5 to 40% by volume xenon, is advantageous especially during long-term ventilation.
- the breathable gas during long-term ventilation has for example a content of from 20 to 30% by volume oxygen, it being possible to increase the oxygen content if required at times for example to 30 to 95% by volume oxygen.
- the remaining gas in the breathable gas usually consists of nitrogen or another inert gas.
- the employed xenon gas generally has the natural isotope composition.
- the isotope composition of the xenon may differ from the natural isotope composition, in particular on use for diagnostic purposes.
- the xenon gas is preferably employed in high purity, as usual for medical gases.
- the xenon gas is preferably used as pure gas or mixed with other gases to produce a gaseous medicament for the applications mentioned.
- Gaseous xenon (pure xenon) is generally provided as compressed gas in compressed gas containers such as compressed gas cylinders or pressurized cans. It is also possible to provide xenon-containing gas mixtures in compressed gas containers.
- the gaseous medicament can also be provided in a container as liquefied gas or gas mixture or in cryogenically solidified form.
- the medicament is usually administered using a ventilation machine with a gas-metering unit or with an anesthesia machine.
- the pharmaceutical is advantageously produced from the pure gases immediately before use, for example by mixing xenon, oxygen and, where appropriate, an inert gas (e.g. with the aid of an anesthesia machine) in the direct vicinity of the patient.
- the medicament is usually administered as dry, moist gas or water vapor-saturated gas to the patient.
- xenon-containing medicament with a medicament which comprises an NO source, preferably for the treatment or prophylaxis of cerebral disorders, in particular for use for cerebral protection.
- the invention thus further relates to a medicament comprising xenon and an NO source or a xenon-containing gas mixture and an NO source, where xenon and NO source are present in pharmacologically effective concentration.
- the invention further relates to a combination product for simultaneous, separate or sequential use of xenon and an NO source or a xenon-containing gas and an NO source.
- the invention relates in particular to a medicament consisting of an inhalable medicament comprising xenon or a xenon-containing gas, and a medicament which is administered preferably orally, by inhalation or parenterally and which comprises an NO source, as combination product for simultaneous, separate or sequential use.
- the invention further relates to the use of xenon and of an NO source or a xenon-containing gas and an NO source for the treatment of cerebral disorders, in particular for cerebral protection.
- the invention further relates to the use of xenon and of an NO source or a xenon-containing gas and an NO source to produce a medicament for the treatment of cerebral disorders, in particular a medicament for cerebral protection.
- the medicament serving as combination product preferably consists of an inhalable medicament comprising xenon or a xenon-containing gas, and of a medicament which is administered orally, by inhalation (e.g. as aerosol) or parenterally and which comprises an NO source.
- a nitric oxide source is NO (nitric oxide), an NO-containing gas or gas mixture or, preferably, a substance or preparation which releases nitric oxide (NO), stimulates endogenous NO production or inhibits the breakdown of NO in the body.
- NO source are, in particular, NO-releasing and/or NO-forming compounds.
- NO sources and, in particular, NO-releasing compounds are described in DE 691 27 756 T2 (e.g. page 8, line 7, to page 9, end of the second paragraph, therein), to which reference is hereby made.
- NO-releasing compounds are S-nitroso-N-acetylpenicillamine (SNAP), S-nitrosocysteine, nitroprusside, nitrosoguanidine, glycerol trinitrate, isoamyl nitrite, inorganic nitrite, azide or hydroxylamine.
- SNAP S-nitroso-N-acetylpenicillamine
- S-nitrosocysteine nitroprusside
- nitrosoguanidine nitrosoguanidine
- glycerol trinitrate isoamyl nitrite, inorganic nitrite, azide or hydroxylamine.
- the NO-releasing compounds are introduced into the lung for example by inhalation as aerosol, as described in DE
- One or more substances stimulating endogenous NO production, one or more NO-releasing compounds and xenon or a xenon-containing gas are thus advantageously administered at separate times or simultaneously.
- a substance stimulating endogenous NO production and, in a further step, NO-releasing compound and xenon are administered.
- NO-releasing compound and xenon are administered.
- xenon by inhalation and, in a further step, to administer the substance stimulating endogenous NO production and an NO-releasing compound, simultaneously or at separate times.
- the combination medicament comprises xenon and at least one NO source in therapeutically effective amount.
- the medicament comprises xenon for example in subanesthetically or anesthetically effective amount.
- the dosage of the substances stimulating endogenous NO production is described for example in WO 00/56328, to which reference is hereby made.
- the dosage of NO-releasing compounds for administration as aerosol is described in U.S. Pat. No. 5,485,827, to which reference is hereby made.
- Medicaments with xenon and an NO source are generally used for the treatment, prophylaxis or prevention of disorders of the brain, especially for cerebral protection.
- the invention thus relates to medicament comprising xenon or a xenon-containing gas and an NO source as combination product for simultaneous, separate or sequential use, especially for disorders of the brain in humans.
- Xenon or xenon-containing gases and an NO source are used to produce a medicament for the treatment, prophylaxis or prevention of impairments of blood flow in the brain, to produce a medicament for the treatment of impairment of cerebral perfusion, to produce a medicament for the treatment of cognitive impairments, to produce a medicament for cerebral protection, to produce a medicament for the prophylaxis and/or therapy of impairments of cognitive performance, also postoperatively, to produce a medicament for the treatment of stroke, to produce a medicament for the prophylaxis of stroke, to produce a medicament for improving the oxygen supply in the brain, to produce a medicament for the treatment of post-ischemia syndrome, to produce a medicament for promoting blood flow in the brain.
- the medicament in a case of stroke the medicament is advantageously employed in the following way. Firstly a xenon-containing gas is administered, e.g. in subanesthetically and sedatively effective amount. In a next phase of the sequential administration of the medicament, advantageously a gaseous, liquid or solid preparation with an NO source (one or more substances to increase the NO level in the brain) or a preparation with an NO source in combination with xenon or a xenon-containing gas is administered.
- an NO source one or more substances to increase the NO level in the brain
- a preparation with an NO source in combination with xenon or a xenon-containing gas is administered.
- Xenon or a xenon-containing gas mixture and an NO source are further used to produce a medicament for the prophylaxis and/or therapy of impairments of cognitive performance, also postoperatively.
- the combination medicament is usually employed as combination of one component (e.g. as inhalable medicament) with xenon and of a further component with an NO source, e.g. a medicament which is administered parenterally, by inhalation or orally and has at least one NO source.
- the medicament comprises xenon in a pharmacologically or therapeutically effective amount, e.g. in subanesthetically or anesthetically effective amount.
- the medicament comprises the NO source in a pharmacologically or therapeutically effective amount.
- the combination medicament consists for example of xenon, an inert gas and an NO source or of xenon, oxygen, an inert gas and an NO source.
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- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Epidemiology (AREA)
- Inorganic Chemistry (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Vascular Medicine (AREA)
- Toxicology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Steroid Compounds (AREA)
Abstract
Description
Claims (7)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/767,604 US7700135B2 (en) | 2000-11-03 | 2007-06-25 | Cerebral protection with a xenon-containing gas |
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10226191 | 2002-06-12 | ||
DE10226191.1 | 2002-06-12 | ||
DE10227975.6 | 2002-06-22 | ||
DE10227975 | 2002-06-22 | ||
DE10236765 | 2002-08-10 | ||
DE10236765.5 | 2002-08-10 | ||
PCT/EP2003/006157 WO2003105871A1 (en) | 2002-06-12 | 2003-06-12 | Cerebral protection with a gas comprising xenon |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/767,604 Division US7700135B2 (en) | 2000-11-03 | 2007-06-25 | Cerebral protection with a xenon-containing gas |
Publications (2)
Publication Number | Publication Date |
---|---|
US20050255168A1 US20050255168A1 (en) | 2005-11-17 |
US7235264B2 true US7235264B2 (en) | 2007-06-26 |
Family
ID=29740361
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/517,723 Expired - Lifetime US7235264B2 (en) | 2000-11-03 | 2003-06-12 | Cerebral protection with a gas comprising xenon |
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US (1) | US7235264B2 (en) |
EP (1) | EP1515732B1 (en) |
JP (1) | JP2005533062A (en) |
CN (1) | CN1668315A (en) |
AT (1) | ATE420650T1 (en) |
AU (1) | AU2003246415A1 (en) |
DE (1) | DE50311092D1 (en) |
DK (1) | DK1515732T3 (en) |
ES (1) | ES2321185T3 (en) |
PT (1) | PT1515732E (en) |
WO (1) | WO2003105871A1 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20100204634A1 (en) * | 2009-02-08 | 2010-08-12 | Blaise Baxter | Devices and methods for perfusion therapy |
US20140155862A1 (en) * | 2009-02-08 | 2014-06-05 | Neuronal Protection System, Llc | Devices and methods for perfusion therapy |
US10369103B2 (en) | 2012-08-10 | 2019-08-06 | The Board Of Regents Of The University Of Texas System | Neuroprotective liposome compositions and methods for treatment of stroke |
US11491184B2 (en) | 2013-03-15 | 2022-11-08 | The Board Of Regents Of The University Of Texas System | Liquids rich in noble gas and methods of their preparation and use |
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FR2964876B1 (en) * | 2010-09-22 | 2013-04-12 | Air Liquide Sante Int | GAS-BASED ANESTHETIC COMPOSITION BASED ON XENON FOR USE DURING CLINICAL ENDARTERIECTOMY OF THE CAROTIDE ARTERY |
US20160030472A1 (en) * | 2013-03-05 | 2016-02-04 | Air Liquide Santé (International) | Xenon-based anesthetic gas composition usable during an endarterectomy involving the clamping of the carotid artery |
FR3022456B1 (en) * | 2014-06-20 | 2016-07-15 | Air Liquide | XENON ASSOCIATED WITH ANTAGONIST OF NMDA RECEPTORS TO FIGHT TUMOR PROLIFERATION IN THE CENTRAL NERVOUS SYSTEM |
KR20210034008A (en) * | 2018-07-18 | 2021-03-29 | 라이크마인즈, 인크. | Method for accelerated tissue penetration of compounds into the brain |
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- 2003-06-12 EP EP03759935A patent/EP1515732B1/en not_active Expired - Lifetime
- 2003-06-12 AU AU2003246415A patent/AU2003246415A1/en not_active Abandoned
- 2003-06-12 AT AT03759935T patent/ATE420650T1/en active
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20100204634A1 (en) * | 2009-02-08 | 2010-08-12 | Blaise Baxter | Devices and methods for perfusion therapy |
US8622992B2 (en) | 2009-02-08 | 2014-01-07 | Blaise Baxter | Devices and methods for perfusion therapy |
US20140155862A1 (en) * | 2009-02-08 | 2014-06-05 | Neuronal Protection System, Llc | Devices and methods for perfusion therapy |
US9526863B2 (en) * | 2009-02-08 | 2016-12-27 | Neuronal Protection System, Llc | Devices and methods for perfusion therapy |
US10369103B2 (en) | 2012-08-10 | 2019-08-06 | The Board Of Regents Of The University Of Texas System | Neuroprotective liposome compositions and methods for treatment of stroke |
US10973764B2 (en) | 2012-08-10 | 2021-04-13 | The Board Of Regents Of The University Of Texas System | Neuroprotective liposome compositions and methods for treatment of stroke |
US11872312B2 (en) | 2012-08-10 | 2024-01-16 | The Board Of Regents Of The University Of Texas Systems | Neuroprotective liposome compositions and methods for treatment of stroke |
US11491184B2 (en) | 2013-03-15 | 2022-11-08 | The Board Of Regents Of The University Of Texas System | Liquids rich in noble gas and methods of their preparation and use |
Also Published As
Publication number | Publication date |
---|---|
EP1515732B1 (en) | 2009-01-14 |
DK1515732T3 (en) | 2009-05-11 |
AU2003246415A1 (en) | 2003-12-31 |
DE50311092D1 (en) | 2009-03-05 |
PT1515732E (en) | 2009-04-14 |
JP2005533062A (en) | 2005-11-04 |
EP1515732A1 (en) | 2005-03-23 |
US20050255168A1 (en) | 2005-11-17 |
CN1668315A (en) | 2005-09-14 |
ATE420650T1 (en) | 2009-01-15 |
WO2003105871A1 (en) | 2003-12-24 |
ES2321185T3 (en) | 2009-06-03 |
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